Clinical Efficacy of Biosimilar Switch of Adalimumab for Management of Uveitis.
dc.contributor.author | Murray, G.M. | |
dc.contributor.author | Griffith, N. | |
dc.contributor.author | Sinnappurajar, P. | |
dc.contributor.author | Al Julandani, D.A. | |
dc.contributor.author | Clarke, S.L.N. | |
dc.contributor.author | Hawley, D.P. | |
dc.contributor.author | Choi, J. | |
dc.contributor.author | Guly, C.M. | |
dc.contributor.author | Ramanan, A.V. | |
dc.date.issued | 2024 | |
dc.description.abstract | Background: Adalimumab has demonstrated efficacy in non-infectious uveitis. With the introduction of biosimilar agents such as Amgevita, we aimed to quantify efficacy and tolerability compared to Humira in a multi-centre UK cohort Methods: Patients identified from tertiary uveitis clinics in 3 centres, after institution-mandated switching was implemented. Results: Data collected for 102 patients, aged 2–75 years, with 185 active eyes. Following switch, rates of uveitis flare were not significantly different (13 events before, 21 after, p = .132). Rates of elevated intraocular pressure were decreased (32 before, 25 afterwards, p = .006) and dosing of oral and intra-ocular steroids was stable. Twenty-four patients (24%) requested to return to Humira, commonly due to pain from injection or technical difficulty with the device. Conclusion: Amgevita is safe and effective for inflammatory uveitis with non-inferiority to Humira. Significant numbers of patients requested to switch back due to side effects including injection site reactions. | |
dc.description.statementofresponsibility | G. M. Murray, N. Griffith, P. Sinnappurajar, D. A. Al Julandani, S. L. N. Clarke, D. P. Hawley, J. Choi, C. M. Guly, Athimalaipet V. Ramanan | |
dc.identifier.citation | Ocular Immunology and Inflammation, 2024; 32(4):442-446 | |
dc.identifier.doi | 10.1080/09273948.2023.2172591 | |
dc.identifier.issn | 0927-3948 | |
dc.identifier.issn | 1744-5078 | |
dc.identifier.orcid | Murray, G.M. [0000-0003-0741-9288] | |
dc.identifier.uri | https://hdl.handle.net/2440/145029 | |
dc.language.iso | en | |
dc.publisher | Taylor and Francis Group | |
dc.rights | © 2023 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. | |
dc.source.uri | https://doi.org/10.1080/09273948.2023.2172591 | |
dc.subject | Adalimumab; biosimilar; clinical efficacy; TNF-alpha; uveitis | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Uveitis | |
dc.subject.mesh | Anti-Inflammatory Agents | |
dc.subject.mesh | Treatment Outcome | |
dc.subject.mesh | Retrospective Studies | |
dc.subject.mesh | Adolescent | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Child | |
dc.subject.mesh | Child, Preschool | |
dc.subject.mesh | Female | |
dc.subject.mesh | Male | |
dc.subject.mesh | Young Adult | |
dc.subject.mesh | Drug Substitution | |
dc.subject.mesh | Biosimilar Pharmaceuticals | |
dc.subject.mesh | Adalimumab | |
dc.title | Clinical Efficacy of Biosimilar Switch of Adalimumab for Management of Uveitis. | |
dc.type | Journal article | |
pubs.publication-status | Published |
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